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TP63相互作用蛋白分析

Bioinformatic Analysis of TP63-related Proteins
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摘要 目的:分析先天缺牙和唇/腭裂综合征相关蛋白--TP63蛋白的相互作用分子,并对其生物学功能进行分析。方法:利用生物信息学数据库(STRING)分析和预测TP63蛋白的相互作用蛋白。在DAVID数据库对相互作用蛋白的生物学功能进行分析。结果:对STRING数据库预测的TP63蛋白50个相互作用蛋白的生物学功能分析显示,TP63相互作用分子主要参与对细胞增殖和凋亡的调节。结论:生物信息学分析初步揭示了TP63蛋白的相互作用网络及其生物学功能。 Objective:To analyze the interactive molecules of TP63 which is related to hypodontia and cleft lip/palate.Methods:The interactive molecules of TP63 were predicted by the STRING database.The molecular biology function was determined by the DAVID database.Results:The STRING database predicted 50 genes that correlated with TP63.Most of them were involved in the cell proliferation and apoptosis process.Conclusion:Bioinformatic analysis tentatively explored the interactive network of TP63 protein.
出处 《口腔医学研究》 CAS CSCD 北大核心 2016年第6期588-591,共4页 Journal of Oral Science Research
基金 国家自然科学基金(编号:81470727 81501750) 湖北省口腔基础医学重点实验室-省部共建国家重点实验室培育基地开放研究基金(编号:201402)
关键词 TP63 相互作用 蛋白质 生物学功能 生物信息学 TP63 Interactive network Protein Biological function Bioinformatics
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参考文献14

  • 1Bamshad M, Jorde LB, Carey JC. Getting a LEAD on EEC [J]. Am J Med Genet, 2000, 90(2)∶183-4.
  • 2Tackels-Horne D, Toburen A, Sangiorgi E, et al. Split hand/split foot malformation with hearing loss: First report of families linked to the SHFM1 locus in 7q21 [J]. Clin Genet, 2001, 59(1)∶28-36.
  • 3Haberlandt E, Loffler J, Hirst-Stadlmann A, et al. Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3 [J]. J Med Genet,2001,38(6)∶405-409.
  • 4O'Quinn JR, Hennekam RC, Jorde LB, et al. Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19 [J]. Am J Hum Genet, 1998, 62(1)∶130-135.
  • 5van Bokhoven H, Jung M, Smits, et al. Limb mammary syndrome:A new genetic disorder with mammary hypoplasia, ectrodactyly,and other hand/foot anomalies maps to human chromosome3q27 [J]. Am J Hum Genet, 1999, 64(2)∶538-546.
  • 6Strano S, Munarriz E, Rossi M, et al. Physical interaction with Yes-associated protein enhances p73 transcriptional activity [J]. J Biol Chem, 2001, 276(18)∶15164-15173.
  • 7Chi S W, Ayed A, Arrowsmith C H. Solution structure of a conserved C-terminal domin of p73 with structural homology to the SAM domain [J]. EMBO J, 1999, 18(16)∶4438-4445.
  • 8Hay RJ, Wells RS. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition [J]. Br J Dermatol, 1976, 94(3)∶277-89.
  • 9Propping, P., Zerres, K. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia [J]. Am J Med Genet, 1993, 45∶642-648.
  • 10Slavotinek AM, Tanaka J, Winder A,et al. Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63 [J]. Am J Med Genet,2005,138A∶146-149.

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